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Cystic Fibrosis DNA detection |
Test |
Cystic Fibrosis DNA detection |
Indication |
The test is indicated for a family with history of cystic fibrosis, the test helps to have a complete family pedigree that includes all medical histories. It is also indicated for prenatal diagnosis in couples known to be carriers. |
Physiology |
Cystic fibrosis is inherited as an autosomal recessive disorder. The gene responsible for the disease has recently been identified and was found to have 250 kilobases and codes for a protein that contains 1480 aminoacids. |
Interpretation |
Alpha fetoprotein, Chloride, Chromosome analysis, Polymerase chain reaction |
Sample |
Laboratory generally provides an interpretive report. |
Test Method |
DNA hybridization |
Related Tests |
Whole blood, amniotic fluid, chorionic villus |
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